Proliferative Verrucous Leukoplakia: A Diagnostic Challenge in a Clinical and Histopathological Context-With Reflections on the Health Reality in Brazil.

Pub Date : 2024-07-08 eCollection Date: 2024-01-01 DOI:10.1155/2024/9166581
Michele Di Benedetto, Gabriela de Figueiredo Meira, Milena Martins da Rocha, Mariel Ruivo Biancardi, Jéssica Barroso Barbosa, Jeconias Câmara, Gerson de Oliveira Paiva Neto, Roberto Luiz de Menezes Martinho, Cássia Maria Fischer Rubira, Silvia Helena de Carvalho Sales Peres
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Abstract

Proliferative verrucous leukoplakia (PVL) is an aggressive and distinct oral disorder with a high potential for malignant transformation (MT). It presents as multifocal lesions that progress over time and frequently recur, often developing carcinomas. Accurately diagnosing PVL is crucial to distinguish it from other oral mucosa lesions that have a lower risk of cancer progression. However, due to the diverse histological features observed in PVL, identifying clinical criteria and histological patterns that can be applied by unfamiliar professionals is challenging. In this study, we present a case of PVL associated with dysplasia in a 53-year-old female patient. The patient exhibited macular and leukoplakic nonscrapable lesions disseminated throughout the oral cavity, with continuous growth. The diagnosis of PVL was established during an 18-month follow-up. This case highlights the difficulties faced by both clinicians and pathologists in diagnosing PVL, emphasizing the need for careful evaluation and accurate diagnosis, particularly in patients with unusual oral lesions, and highlighting the discrepancies observed in the application of available protocols to our particular case. Distinguishing PVL from similar conditions can be challenging due to overlapping clinical signs and indistinct histopathological features.

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增生性疣状白斑病:临床和组织病理学背景下的诊断难题--对巴西卫生现实的思考。
增殖性疣状白斑病(PVL)是一种侵袭性的独特口腔疾病,极易发生恶性转化(MT)。它表现为多灶性病变,随着时间的推移,病变会不断发展,并经常复发,通常会发展成癌。要将 PVL 与其他癌变风险较低的口腔黏膜病变区分开来,准确诊断 PVL 至关重要。然而,由于在 PVL 中观察到的组织学特征多种多样,因此确定可供陌生专业人员应用的临床标准和组织学模式具有挑战性。在本研究中,我们介绍了一例 53 岁女性患者伴有发育不良的 PVL 病例。患者口腔各处散布着斑丘疹和白斑性非刮除性病变,且持续增长。在 18 个月的随访中确诊为 PVL。本病例凸显了临床医生和病理学家在诊断 PVL 时所面临的困难,强调了仔细评估和准确诊断的必要性,尤其是对于口腔异常病变的患者,并强调了在我们的特殊病例中应用现有方案时所观察到的差异。由于临床症状重叠和组织病理学特征不明确,将 PVL 与类似病症区分开来可能具有挑战性。
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